Fact-checked by Grok 2 weeks ago

Weakness

Weakness is the quality or state of being weak, defined as a lack of strength, vigor, or power, which can apply to physical, mental, moral, or structural contexts, and may also denote a fault, defect, or vulnerability in individuals, materials, or systems.^[1] In medicine, weakness typically refers to a reduction in muscle strength or overall bodily vigor, often presenting as generalized fatigue or localized impairment, and serves as a common symptom of underlying conditions such as stroke, multiple sclerosis, infections, nutritional deficiencies, or electrolyte imbalances. It is distinct from fatigue, though the two may overlap, with weakness involving an objective decrease in force generation rather than subjective tiredness alone.^[2] Diagnosis requires distinguishing true muscle weakness from pain-related limitations or perceived debility through clinical evaluation, including history, physical examination, and targeted testing.^[3]

Definition and Classification

Definition

In medicine, weakness is defined as a loss of muscle strength, characterized by a reduced capacity of one or more skeletal muscles to generate the expected force or power output during voluntary contraction. This symptom can be localized to specific muscle groups or generalized across the body and is evaluated objectively through standardized techniques such as manual muscle testing on a 0-5 scale or dynamometry using hand-held devices to quantify maximal isometric strength, while subjective assessment relies on patient-reported difficulties in performing routine tasks.^[4]^[5]^[6] True weakness differs fundamentally from normal fatigue, which represents a reversible state of diminished performance following prolonged exertion or inadequate recovery, typically resolving with rest without altering baseline muscle power. In contrast, weakness indicates a pathological impairment where maximal voluntary effort fails to produce normal force, often persisting independently of rest and signaling disruption in neuromuscular function.^[7]^[8] Clinically, weakness serves as a frequent presenting symptom in primary care, where it constitutes a common complaint among patients seeking evaluation for functional limitations, and in emergency settings, where it may herald acute, life-threatening conditions such as stroke, infection, or electrolyte imbalances. Affecting approximately 5% of adults aged 60 years and older in the United States based on criteria for weak muscle strength from the 2011-2012 National Health and Nutrition Examination Survey (NHANES), weakness substantially impairs quality of life by restricting mobility, independence in daily activities, and overall physical functioning, thereby underscoring the need for timely assessment to mitigate long-term disability.^[7]^[9]

Types of Weakness

Weakness in clinical medicine is broadly classified into several subtypes based on its objective measurability, subjective experience, and patterns of fatigability or generalization. True weakness refers to an objective loss of muscle power, verifiable through physical examination, such as the inability to generate sufficient force to overcome gravity in affected limbs.^[7] This contrasts with perceived weakness, which involves a subjective sensation of reduced strength without demonstrable loss on testing, often arising from psychological factors or deconditioning.^[10] Asthenia represents a generalized feeling of bodily weakness that is not confined to specific muscle groups, commonly observed in the context of chronic illnesses where patients report an overall debility rather than localized impairment.^[11] In distinction, myasthenia denotes a specific form of fatigable weakness, characterized by muscle power that diminishes with repeated use and recovers with rest, as exemplified by the fluctuating symptoms in myasthenia gravis affecting ocular or bulbar muscles.^[12] Fatigue-based types of weakness further delineate based on the site of predominant dysfunction. Central weakness originates from brainstem or cortical levels, leading to profound tiredness that limits sustained effort, such as in multiple sclerosis where patients experience exacerbated exhaustion with activity.^[4] Neuromuscular weakness involves failure at the neuromuscular junction, resulting in transmission-related fatigability that impairs repetitive actions.^[7] Peripheral weakness stems from muscle fiber dysfunction, manifesting as localized power deficits that worsen with exertion but are distinct from central origins.^[10]

Clinical Presentation

Symptoms

Patients commonly describe muscle weakness subjectively as a sensation of heaviness or fatigue in the affected limbs, often reporting that they tire easily during routine activities or feel unable to perform familiar tasks, such as climbing stairs or lifting objects.^[5] This subjective experience is distinguished from general tiredness by its specific impact on motor function, where patients note a progressive decline in their ability to sustain effort.^[7] Objectively, weakness manifests as measurable reductions in muscle power, such as diminished grip strength when squeezing an examiner's hand, instability in gait leading to stumbling or falls, or visible drooping of the eyelids (ptosis) in cases involving facial or ocular muscles.^[7] These signs are typically elicited during physical examination and help quantify the extent of impairment beyond patient reports.^[5] While weakness frequently co-occurs with associated symptoms like localized pain during muscle use, sensory numbness, or unexplained weight loss, the core descriptors remain centered on motor limitations, including rapid fatigability and reduced endurance in repetitive movements.^[7] These accompanying features provide context but do not define the primary complaint of diminished strength.^[5] The functional impact of weakness profoundly disrupts activities of daily living (ADLs), such as difficulty dressing due to inability to raise arms overhead or challenges in walking that necessitate assistive devices.^[7] Clinicians often assess severity using the Medical Research Council (MRC) scale for muscle strength, a validated 0-5 grading system where 0 indicates no visible contraction, 3 represents movement against gravity but not resistance, and 5 denotes normal power against full resistance.^[6] This scale enables standardized evaluation of how weakness compromises independence in tasks like self-care or mobility.^[13]

Patterns of Weakness

Weakness patterns in clinical practice are characterized by the distribution and temporal evolution of muscle involvement, which help clinicians localize the underlying issue to specific neural or muscular structures. Proximal weakness predominantly affects the muscles of the shoulder and hip girdles, such as difficulty rising from a chair or combing hair, and is commonly observed in conditions involving the muscle fibers themselves, like inflammatory myopathies.^[14] In contrast, distal weakness involves the extremities farther from the torso, such as impaired fine finger movements or foot drop, and is more typical in disorders affecting peripheral nerves, where involvement starts in the hands and feet.^[15] Symmetry in weakness distribution further refines localization, with bilateral symmetric patterns often indicating widespread processes affecting both sides equally, such as in systemic inflammatory or toxic conditions that impact muscles or nerves diffusely.^[16] Asymmetric weakness, however, suggests focal pathology, including unilateral involvement on one side of the body, as seen in vascular events disrupting localized neural pathways.^[17] The tempo of progression distinguishes acute from chronic patterns; sudden acute weakness develops rapidly over minutes to hours, often pointing to central vascular or traumatic events, while subacute progressive weakness over days to weeks, reaching peak severity within two weeks, suggests inflammatory or immune-mediated processes affecting the peripheral nervous system, such as Guillain-Barré syndrome.^[18] Chronic patterns, by comparison, evolve gradually over months to years, with insidious worsening that may include periods of stability, characteristic of degenerative conditions involving motor neurons.^[19] Fatigability refers to weakness that worsens with repeated muscle use and improves with rest, a hallmark of disorders at the neuromuscular junction where transmission fatigues under sustained activity.^[20] Non-fatigable weakness remains relatively constant regardless of repetition, as occurs in structural disruptions like vascular lesions, where the deficit stems from fixed neural damage rather than dynamic failure.^[21]

Pathophysiology

Central Mechanisms

Central mechanisms of weakness originate in the central nervous system (CNS), encompassing the brain and spinal cord, where disruptions impair the neural drive to muscles without directly affecting peripheral neuromuscular junctions. Upper motor neurons (UMNs), particularly those in the corticospinal tracts, play a pivotal role in initiating and modulating voluntary movement. Lesions or dysfunction in these tracts lead to spastic weakness, characterized by increased muscle tone, hyperreflexia, and pathological reflexes such as the Babinski sign, due to the loss of inhibitory control over lower motor neurons.^[22]^[4] This spasticity arises from the disinhibition of spinal reflex arcs, resulting in velocity-dependent resistance to passive movement and a characteristic pattern of weakness that is more pronounced in antigravity muscles.^[23] Central fatigue represents another key CNS-driven process, involving diminished motivational drive and reduced neural output from higher brain centers, often linked to imbalances in neurotransmitters. Elevated serotonin levels relative to dopamine in the brain can contribute to this fatigue by altering the perception of effort and suppressing motor cortex excitability, as observed in conditions involving prolonged exertion.^[24] Dopamine depletion, in particular, impairs reward processing and sustained activation of motor pathways, leading to a subjective sense of exhaustion despite intact peripheral muscle function.^[25] These imbalances disrupt the supraspinal regulation of motor commands, manifesting as a progressive decline in force generation during repeated efforts.^[26] Contributions from the brainstem and cerebellum further elucidate CNS mechanisms, where coordination failures produce ataxia-like weakness. Cerebellar dysfunction interrupts the fine-tuning of motor commands, resulting in impaired timing and precision of movements that mimic weakness through ineffective force application and tremor.^[27] Brainstem lesions, affecting pathways like the rubrospinal or reticulospinal tracts, exacerbate this by altering postural stability and excitatory drive to spinal motor pools, leading to dysmetria and intention tremor that compound the perception of limb debility.^[28] At a quantitative level, central mechanisms often involve failures in motor unit recruitment, where the CNS inadequately activates available motor units to meet force demands. In healthy neural signaling, motor units are recruited in an orderly manner based on the size principle, starting with smaller, fatigue-resistant units and progressing to larger ones for greater force.^[29] Disruptions in corticospinal volleys reduce the efficiency of this recruitment, leading to suboptimal firing rates and incomplete activation of the motor pool, as evidenced by decreased electromyographic (EMG) activity during maximal efforts.^[30] This central inefficiency highlights the CNS's role in scaling muscle activation without peripheral fatigue.

Peripheral Mechanisms

Peripheral mechanisms of weakness involve disruptions at the level of the lower motor neurons, peripheral nerves, neuromuscular junction, and muscle fibers themselves, leading to impaired force generation distinct from central nervous system origins. In lower motor neuron lesions, denervation occurs when motor neurons fail to innervate muscle fibers, resulting in flaccid weakness characterized by reduced muscle tone and hyporeflexia. This denervation triggers rapid muscle atrophy due to the absence of neural trophic support, with affected muscles exhibiting fibrillations and fasciculations as denervated fibers become hyperexcitable.^[31]^[32]^[33] Axonal transport failure in peripheral nerves exacerbates this process by impairing the delivery of essential proteins, organelles, and neurotrophic factors to distal axons, leading to axonal degeneration and subsequent denervation. For instance, disruptions in anterograde or retrograde transport, as seen in toxic neuropathies or hereditary motor neuropathies, cause neurofilament accumulation, axonal swelling, and distal axonopathy, culminating in progressive weakness and atrophy.^[34] At the neuromuscular junction, defects such as acetylcholine receptor blockade impair synaptic transmission, producing fatigable weakness that worsens with repeated activity. In myasthenia gravis, autoantibodies target postsynaptic acetylcholine receptors, reducing their density through complement-mediated destruction and internalization, which diminishes the endplate potential and safety factor of neuromuscular transmission. This leads to incomplete muscle activation and rapid fatigue during sustained or repetitive contractions.^[35] Muscle fiber pathology contributes to weakness through either energy metabolism failures or structural damage. In metabolic myopathies, enzymatic defects in glycogenolysis, fatty acid oxidation, or mitochondrial function cause ATP depletion during exercise, preventing cross-bridge cycling and leading to acute weakness and exercise intolerance. For example, deficiencies in phosphorylase or carnitine palmitoyltransferase result in rapid fatigue due to insufficient energy substrates for contraction.^[36]^[37] Structural defects, such as the absence of dystrophin in Duchenne muscular dystrophy, destabilize the sarcolemma, making muscle fibers susceptible to mechanical stress and calcium influx, which triggers necrosis, inflammation, and progressive weakness with fiber replacement by fibrofatty tissue.^[38] Peripheral fatigue arises from local ionic imbalances during prolonged muscle activity, independent of central drive. Potassium efflux from muscle fibers during repeated contractions elevates extracellular potassium concentrations in the t-tubules, depolarizing the membrane and inactivating sodium channels, which blocks action potential propagation and reduces force output. This mechanism contributes to the decline in muscle performance, particularly in high-intensity efforts, by disrupting excitation-contraction coupling.^[39]^[40]

Causes

Neurological Causes

Neurological causes of weakness primarily involve disorders of the central nervous system (CNS) or peripheral nervous system (PNS), leading to disruption of motor pathways and resulting in various patterns of muscle impairment. These etiologies often present with focal or symmetric weakness, depending on the site of involvement, and require prompt evaluation to distinguish from other causes. Stroke and transient ischemic attacks (TIAs) represent acute ischemic events in the brain that commonly cause sudden focal weakness, such as hemiparesis affecting one side of the body. In ischemic stroke, occlusion of cerebral arteries leads to infarction in motor areas, resulting in contralateral weakness that may include facial droop and limb paresis; TIAs produce similar transient symptoms resolving within 24 hours due to temporary hypoperfusion.^[41]^[42] These conditions account for a significant portion of acute weakness presentations in emergency and neurology settings, with hemiparesis occurring in approximately 80% of acute stroke cases.^[43] Multiple sclerosis (MS) is an autoimmune demyelinating disease of the CNS that leads to relapsing-remitting episodes of weakness due to inflammation and loss of myelin in white matter tracts. This process disrupts nerve conduction in motor pathways, causing transient focal or generalized weakness, often accompanied by sensory changes or fatigue; the relapsing-remitting form, the most common initial presentation, features episodes of symptom exacerbation followed by partial or full recovery.^[44]^[45] Amyotrophic lateral sclerosis (ALS) involves progressive degeneration of upper and lower motor neurons in the CNS and PNS, leading to insidious onset of muscle weakness that spreads from distal limbs to proximal muscles and bulbar regions. Pathophysiologically, the loss of motor neurons results in denervation atrophy, fasciculations, and eventual respiratory compromise, with weakness typically asymmetric at onset but becoming generalized over time.^[46] Myasthenia gravis is an autoimmune disorder affecting the neuromuscular junction, leading to fatigable weakness that worsens with activity and improves with rest, often involving ocular, bulbar, and proximal limb muscles due to autoantibodies against acetylcholine receptors.^[7] Guillain-Barré syndrome, an acute post-infectious autoimmune polyneuropathy, causes rapid symmetric ascending weakness starting in the lower limbs, potentially progressing to respiratory involvement, mediated by demyelination or axonal damage in peripheral nerves.^[7] Peripheral neuropathies, including diabetic and inflammatory types such as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), cause symmetric distal weakness through damage to peripheral nerves. In diabetic neuropathy, chronic hyperglycemia leads to axonal degeneration, manifesting as stocking-glove distribution sensory loss and weakness starting in the feet; CIDP, an immune-mediated demyelinating disorder, produces proximal and distal symmetric weakness that progresses over weeks to months, often responsive to immunotherapy.^[47]^[48] Neurological causes constitute a substantial proportion of weakness evaluations in outpatient neurology clinics, often requiring electrodiagnostic studies for confirmation.^[7]

Musculoskeletal Causes

Musculoskeletal causes of weakness primarily arise from disorders affecting the muscles, tendons, bones, or joints directly, leading to impaired muscle function or structural limitations that reduce strength. These conditions often present with localized or symmetrical weakness, distinguishable from neural or systemic origins by their focus on tissue-level pathology. Common examples include myopathies, electrolyte disturbances impacting muscle excitability, atrophy from injury or inactivity, and joint-related instabilities. Myopathies, disorders of skeletal muscle, are a leading musculoskeletal cause of weakness, characterized by intrinsic muscle damage or dysfunction. Inflammatory myopathies, such as polymyositis, involve autoimmune-mediated inflammation of muscle fibers, resulting in symmetrical proximal weakness affecting the shoulders, hips, and thighs, often progressing over weeks to months.^[49] Genetic myopathies, exemplified by Duchenne muscular dystrophy, stem from mutations in genes like DMD, leading to progressive proximal muscle weakness that typically begins in early childhood, with initial involvement of pelvic and shoulder girdle muscles, causing difficulties in walking, climbing stairs, and rising from a seated position.^[50] These myopathies disrupt muscle fiber integrity and contractility, often without sensory loss, and may briefly intersect with peripheral mechanisms through impaired excitation-contraction coupling.^[51] Electrolyte imbalances, particularly hypokalemia (serum potassium below 3.5 mEq/L), can precipitate acute muscle weakness by altering membrane potentials and impairing muscle cell depolarization, sometimes manifesting as flaccid paralysis. In severe cases, hypokalemia triggers episodes of generalized weakness or paralysis, often reversible with potassium repletion, and is frequently linked to dietary deficiencies, gastrointestinal losses, or medications like diuretics.^[52] Trauma and disuse contribute to weakness through muscle atrophy, where prolonged immobilization or injury reduces muscle protein synthesis and promotes breakdown, leading to measurable strength loss. Post-injury atrophy, common after fractures or soft tissue damage, can lead to significant atrophy within weeks of immobility, resulting in reversible weakness that improves with rehabilitation.^[53] Disuse from casting or bed rest similarly induces atrophy via reduced mechanical loading, exacerbating weakness in affected limbs.^[54] Osteoarticular disorders, such as arthritis, often mimic or exacerbate muscle weakness through joint inflammation, pain, and instability that limit effective muscle use. In osteoarthritis, degenerative changes in joints like the knee or hip lead to surrounding muscle weakness, with studies showing up to 19% reduction in quadriceps cross-sectional area due to disuse and inflammation, creating a cycle of instability and perceived weakness.^[55] Rheumatoid arthritis similarly causes joint laxity and erosions, contributing to proximal weakness in the upper and lower extremities by compromising biomechanical support for muscle action.^[56]

Systemic Causes

Systemic causes of weakness encompass a range of non-neuromuscular disorders that affect the body broadly, leading to generalized fatigue and reduced muscle performance through mechanisms such as metabolic disruption, inflammation, or nutritional deficits. These conditions often present with asthenia, a subjective sense of profound tiredness and weakness that impairs daily activities, and they are particularly prevalent in older adults where multiple factors like chronic inflammation and comorbidities contribute to multifactorial etiology.^[7]^[57] Endocrine disorders, notably thyroid dysfunction, frequently manifest as generalized weakness. Hypothyroidism, characterized by insufficient thyroid hormone production, leads to hypothyroid myopathy, which causes proximal muscle weakness, cramps, and stiffness due to impaired energy metabolism in muscle fibers.^[58]^[59] In contrast, hyperthyroidism, often from Graves' disease, results in thyrotoxic myopathy with proximal weakness, muscle wasting, and asthenia, exacerbated by increased catabolism and electrolyte imbalances.^[60]^[61] Infectious diseases can induce weakness through persistent systemic effects. Post-viral fatigue syndromes, following infections like Epstein-Barr virus or SARS-CoV-2, produce prolonged muscle weakness and exhaustion that worsen with exertion, linked to immune dysregulation and mitochondrial dysfunction.^[62]^[63] Bacterial infections such as Lyme disease, caused by Borrelia burgdorferi, may lead to peripheral neuropathy with associated limb weakness and sensory loss, stemming from neuroborreliosis affecting nerve function.^[64]^[65] Metabolic imbalances are key contributors to weakness via reduced oxygen delivery or neural integrity. Anemia, particularly iron-deficiency or chronic disease-related types, diminishes hemoglobin levels, causing tissue hypoxia that manifests as profound fatigue and generalized weakness.^[66]^[67] Vitamin B12 deficiency triggers subacute combined degeneration of the spinal cord, resulting in demyelination of posterior and lateral columns, which produces progressive limb weakness, ataxia, and paresthesias.^[68]^[69] Malignancies contribute to weakness through paraneoplastic syndromes or cachexia. Paraneoplastic processes, such as Lambert-Eaton myasthenic syndrome associated with small-cell lung cancer, cause proximal muscle weakness and fatigability due to autoantibodies targeting neuromuscular junctions.^[70]^[71] Cancer cachexia, a wasting syndrome in advanced tumors, involves severe muscle loss, weakness, and fatigue from cytokine-driven inflammation and metabolic alterations, affecting up to 80% of patients with progressive disease.^[72]^[73]

Diagnosis

History and Examination

The evaluation of weakness begins with a detailed patient history to characterize the symptom and guide subsequent physical examination. Key elements include the onset, which may be acute (suggesting vascular events like stroke or infectious processes), subacute (implicating toxic, metabolic, or inflammatory etiologies), or chronic progressive (pointing toward hereditary or degenerative conditions).^[74] Duration helps differentiate transient episodes from persistent deficits, while the anatomic distribution—such as symmetric proximal involvement (e.g., difficulty rising from a chair) versus asymmetric or distal patterns—provides clues to underlying mechanisms, including potential patterns of weakness like pyramidal or neuromuscular junction disorders.^[74] Exacerbating or alleviating factors are also elicited, such as fatigability worsened by repetitive activity or later in the day, which is characteristic of myasthenia gravis.^[74] Physical examination focuses on systematic assessment of muscle power, tone, and coordination to localize the lesion. Strength is graded using the Medical Research Council (MRC) scale, a standardized 0-5 ordinal system where grade 0 indicates no contraction, 1 is flicker or trace contraction without movement, 2 is movement with gravity eliminated, 3 is movement against gravity but not resistance, 4 is movement against some resistance, and 5 is normal power against full resistance.^[6] This is applied to major muscle groups bilaterally, starting proximally and comparing sides for asymmetry. Reflex testing evaluates deep tendon reflexes (e.g., biceps, patellar) on a 0-4 scale (0 absent, 4+ clonus), with hyperreflexia suggesting upper motor neuron involvement and hyporeflexia indicating lower motor neuron or peripheral issues. The sensory examination assesses light touch, pinprick, vibration, and proprioception in dermatomal distributions to identify concurrent neuropathy or radiculopathy contributing to perceived weakness.^[75] Additional maneuvers include observing for pronator drift (arm weakness) or heel-toe walking deficits (distal lower limb involvement). Certain features in the history and examination warrant urgent attention as red flags. Sudden onset unilateral weakness, often with facial droop or arm drift, raises concern for ischemic stroke requiring immediate intervention.^[76] Progressive bulbar symptoms, such as dysphagia, dysarthria, or tongue weakness, signal possible amyotrophic lateral sclerosis (ALS), particularly if accompanied by upper and lower motor neuron signs like fasciculations.^[77] Objective functional assessments quantify the impact of weakness on daily activities. The Timed Up and Go (TUG) test measures mobility by timing the sequence of rising from a chair, walking 3 meters, turning, returning, and sitting; times exceeding 13.5 seconds indicate increased fall risk and mobility impairment due to lower limb weakness.^[78] The 6-minute walk test (6MWT) evaluates endurance by recording the distance covered on a flat course at self-selected pace, with rests allowed; reduced distances (e.g., <300 meters in adults) reflect submaximal capacity limited by proximal or generalized weakness in conditions like myopathy or neuropathy.^[79] These tests complement bedside findings by providing measurable outcomes tied to observed patterns of weakness.

Differential Diagnosis

The differential diagnosis of weakness begins with distinguishing true muscle weakness, characterized by objective loss of motor power, from perceived or subjective weakness, where patients report fatigue or effort without measurable deficit. True weakness is confirmed through objective assessments such as the Medical Research Council (MRC) Manual Muscle Testing scale, which grades strength from 0 (no contraction) to 5 (normal power against resistance), revealing deficits in specific muscle groups.^[7] In contrast, perceived weakness often stems from non-neuromuscular factors like depression, chronic fatigue syndrome, or deconditioning, and requires psychological evaluation to identify functional components, such as inconsistent effort or give-way weakness during exam.^[4] Electromyography (EMG) further supports differentiation by detecting abnormalities in muscle or nerve function indicative of true pathology, absent in purely subjective cases.^[4] A key distinction arises between asthenia, a general sense of fatigue or debility without fatigability, and myasthenia, as in myasthenia gravis, where weakness worsens with repetitive activity and improves with rest. Asthenia may reflect systemic issues like anemia or hypothyroidism, lacking the fluctuating pattern seen in myasthenia gravis, which typically involves ocular or bulbar muscles initially.^[7] Endurance tests, such as sustained upward gaze for 30 seconds or repetitive handgrip, help differentiate: in myasthenia, ptosis or grip strength declines progressively, while asthenia shows stable but reduced baseline effort.^[80] Repetitive nerve stimulation (RNS) at 2-3 Hz confirms myasthenia by demonstrating a ≥10% decrement in compound muscle action potential, a finding not seen in asthenia.^[80] Investigative tools are selected based on clinical suspicion to narrow the differential. Blood tests include creatine kinase (CK) levels, which elevate in myopathies (e.g., >5 times upper limit in inflammatory or toxic forms), and electrolytes like potassium, as hypokalemia can mimic proximal weakness.^[81] Thyroid-stimulating hormone (TSH) screens for endocrine causes, while EMG/nerve conduction studies (NCS) localize lesions: myopathic changes (small, polyphasic potentials) suggest muscle disorders, whereas neuropathic patterns indicate peripheral nerve issues.^[7] MRI of the brain or spine is prioritized for asymmetric or acute weakness to detect central lesions, such as stroke or demyelination, guiding further confirmatory tests like biopsy if needed.^[4] Common pitfalls in diagnosis include overlooking functional disorders, where patients exhibit non-anatomic weakness patterns responsive to suggestion, or medication side effects, such as statin-associated muscle symptoms (SAMS) in approximately 5-20% of users, with confirmed myopathy (often with elevated CK and proximal symptoms) being less common (1-5%).^[81]^[82] Glucocorticoids can exacerbate weakness through steroid myopathy, often with normal CK, necessitating medication review early in evaluation.^[81] An algorithmic approach to differential diagnosis proceeds stepwise: (1) Elicit history for onset, distribution (proximal vs. distal, symmetric vs. asymmetric), and associated symptoms (e.g., fatigability suggesting neuromuscular junction disorder); (2) Perform targeted exam with MRC grading and endurance testing to confirm objective weakness; (3) Order initial labs (CK, electrolytes, TSH) and, if indicated, EMG/NCS to classify as myopathic, neuropathic, or central; (4) Use MRI for focal deficits and consider specialist referral (e.g., neurology) or advanced testing (e.g., autoantibody panels) if initial results are inconclusive; (5) Reassess for pitfalls like drugs or psychological factors before proceeding to invasive diagnostics.^[7] This structured process minimizes misdiagnosis and ensures efficient progression to confirmatory studies.^[4]

Management

Initial Assessment

The initial assessment of a patient presenting with weakness prioritizes stabilization to address life-threatening complications, beginning with evaluation of the airway, breathing, and circulation (ABCs). In acute settings, such as the emergency department, clinicians must rapidly assess for respiratory compromise, particularly in conditions involving neuromuscular involvement like Guillain-Barré syndrome (GBS), where up to 25% of patients develop respiratory insufficiency requiring mechanical ventilation. Vital signs, including blood pressure, heart rate, and oxygen saturation, should be monitored closely for signs of autonomic instability, such as tachycardia or hypertension, which can occur in progressive weakness syndromes.^[83]^[84] Risk stratification follows ABC stabilization to identify patients needing urgent intervention, focusing on red flags such as bulbar involvement (e.g., dysphagia or dysarthria), rapid progression over hours to days, or bilateral symmetric weakness suggesting peripheral causes. For instance, in GBS, characterized by ascending weakness and hyporeflexia, immediate triage to intensive care is warranted if vital capacity falls below 20 mL/kg or if there is a 50% daily decline, as these indicate impending respiratory failure. Patients with these features should be referred urgently to neurology or critical care for further evaluation, while those with stable, non-progressive weakness may undergo outpatient follow-up.^[83]^[84] Supportive care during initial assessment aims to prevent secondary complications, including provision of intravenous hydration to maintain fluid balance and avoid dehydration, which can exacerbate muscle weakness in neuromuscular disorders. Nutritional support, such as early enteral feeding within 24-48 hours for patients at risk of dysphagia, helps preserve muscle mass and prevent malnutrition, with energy targets around 30 kcal/kg body weight recommended for non-ventilated individuals. Mobility aids, like canes or wheelchairs, should be provided promptly to reduce fall risk, especially in elderly or deconditioned patients with lower extremity weakness.^[85]^[83] Ongoing monitoring in acute settings involves serial neurological examinations every 4-6 hours to track weakness progression, alongside repeated assessments of respiratory function using tools like vital capacity measurements or single-breath counts. This allows for timely escalation of care, such as non-invasive ventilation trials in stable patients with diaphragmatic involvement, ensuring dynamic adjustment to the patient's evolving status.^[84]^[83]

Therapeutic Approaches

Therapeutic approaches to weakness prioritize addressing the underlying etiology to restore muscle function and improve quality of life, with treatments ranging from pharmacological agents to rehabilitative and supportive interventions. Evidence-based strategies are tailored to specific causes, such as inflammatory, neuromuscular, or systemic disorders, and often combine multiple modalities for optimal outcomes.^[86] Pharmacological treatments target disease-specific mechanisms to alleviate weakness. In inflammatory myopathies like polymyositis and dermatomyositis, first-line therapy typically involves corticosteroids such as prednisone, often combined with immunosuppressants including methotrexate or azathioprine to reduce inflammation and muscle damage; these agents have demonstrated efficacy in improving strength and function in responsive patients.^[87]^[88] For myasthenia gravis, a neuromuscular junction disorder, pyridostigmine—an acetylcholinesterase inhibitor—is the cornerstone symptomatic treatment, enhancing acetylcholine availability to counteract fatigable weakness; it is generally safe for long-term use and improves daily function in most patients.^[89]^[90] Disease-modifying therapies aim to halt or slow progression in acute or neurodegenerative conditions. For acute inflammatory neuropathies such as Guillain-Barré syndrome, intravenous immunoglobulin (IVIG) or plasmapheresis is recommended as first-line treatment to remove pathogenic antibodies and accelerate recovery from paralysis and weakness; randomized trials show both modalities reduce disability at four weeks with comparable efficacy, though IVIG is often preferred for ease of administration.^[91] In amyotrophic lateral sclerosis (ALS), riluzole—a glutamate release inhibitor—extends survival by approximately three months on average when initiated early, modestly slowing motor neuron degeneration and weakness progression. Additional approved therapies include edaravone, an antioxidant that slows functional decline in early-stage ALS, and tofersen, an antisense oligonucleotide for patients with SOD1 gene mutations that reduces disease progression markers.^[92]^[93]^[94]^[95] Rehabilitative interventions focus on preserving and rebuilding muscle strength through structured exercise protocols. Physical therapy, particularly resistance training, effectively counters disuse atrophy by stimulating muscle protein synthesis and increasing strength; meta-analyses of randomized controlled trials confirm that progressive resistance exercises mitigate muscle loss during immobilization, with gains in mass and function observed in both younger and older adults.^[96]^[97] Supportive measures enhance mobility and prevent complications from weakness. Orthotics, such as ankle-foot orthoses (AFOs), provide stability for lower limb weakness, improving gait and reducing fall risk in conditions like peripheral neuropathy or post-stroke deficits; clinical studies support their use in compensating for plantar flexion weakness without substituting for active rehabilitation.^[98] Nutritional supplementation addresses deficiency-related causes, as in osteomalacia where vitamin D therapy—typically 50,000 IU weekly initially—reverses proximal muscle weakness by promoting bone and muscle health; treatment normalizes serum levels and alleviates symptoms within months.^[99]^[100] Prognosis for weakness varies markedly by cause, influencing therapeutic expectations. Electrolyte imbalances, such as hypokalemia or hypophosphatemia, often lead to reversible weakness that resolves rapidly with correction, restoring full strength without residual deficits in most cases.^[101] In contrast, ALS presents a progressive course where weakness advances despite riluzole and supportive care, with median survival of 2–5 years from symptom onset and limited functional recovery.^[93] Overall, multidisciplinary approaches improve outcomes in treatable etiologies, emphasizing early intervention to maximize reversibility.^[86]

References

[1]
WEAKNESS Definition & Meaning - Merriam-Webster
Nov 1, 2025 · 1. The quality or state of being weak; also : an instance or period of being weak; backed down in a moment of weakness. 2. Fault, defect.
[2]
Weakness and Fatigue - PubMed
Weakness refers to a decrease in muscle strength. Fatigue is tiredness that may be either independent of, or associated with, exertion.
[3]
Muscle Weakness in Adults: Evaluation and Differential Diagnosis
Jan 15, 2020 · True muscle weakness must first be differentiated from subjective fatigue or pain-related motor impairment with normal motor strength.<|separator|>
[4]
Weakness of Will - jstor
second, do we have weak-willed behaviour-the first is reckless- ness, and the third is compulsion. ' Secondly, it is not necessary. Weakness of will can be the.
[5]
SKEPTICISM ABOUT WEAKNESS OF WILL* Gary Watson - jstor
A Though it occurs with deplorable frequency, weakness of will has seemed to many philosophers hard to understand. The motivation of weak behavior' is generally ...
[6]
Assessing weak shear capacity in unreinforced prestressed ... - ASCE
Jul 25, 2022 · Despite having high flexural capacity, PCHC slabs have shown relatively weak shear capacity, which is attributed to the limitations of the ...
[7]
https://www.aafp.org/pubs/afp/issues/2020/0115/p95.html
[8]
Structural Building Condition Surveys: Looking for Trouble - ASCE
Realize the importance of a careful structural inspection program during construction; Learn structural weaknesses and limitations of some common building ...
[9]
FRAILTY Definition & Meaning - Merriam-Webster
1. The quality or state of being frail; the frailty of her health; the frailty and disability in the elderly. 2. A fault due to weakness especially of moral ...
[10]
WEAKNESSES Synonyms: 34 Similar and Opposite Words
Synonyms for WEAKNESSES: faults, shortcomings, sins, deficiencies, failings, frailties, foibles, vices; Antonyms of WEAKNESSES: virtues, merits, perfections ...
[11]
Weakness - Neurologic Disorders - Merck Manual Professional Edition
Weakness is loss of muscle strength, although many patients also use the term when they feel generally fatigued or have functional limitations.
[12]
Muscle Weakness Causes & Treatment - Cleveland Clinic
Feb 12, 2025 · Muscle weakness is when your muscles can't work with the expected amount of force. It's a common symptom, and many of the causes are ...
[13]
Muscle Strength Grading - StatPearls - NCBI Bookshelf
Apr 27, 2025 · Dynamometry reduces examiner subjectivity, enhancing consistency in measuring muscle strength changes over time.
[14]
Muscle Weakness in Adults: Evaluation and Differential Diagnosis
Jan 15, 2020 · True muscle weakness must first be differentiated from subjective fatigue or pain-related motor impairment with normal motor strength.
[15]
Weakness and fatigue: Understanding the difference | Parkview Health
Jun 20, 2023 · Generally speaking, weakness is a lack of physical or muscle strength. When experiencing body weakness, you feel like you need to use extra ...
[16]
Evaluation of the Patient with Muscle Weakness - AAFP
Apr 1, 2005 · Muscle weakness is a common complaint among patients presenting to family physicians. Diagnosis begins with a patient history distinguishing ...
[17]
Emergency department patients with weakness or fatigue
Nov 5, 2020 · Generalized weakness and fatigue are underexplored symptoms in emergency medicine. Triage tools often underestimate patients presenting to the emergency ...
[18]
Asthenia (weakness): Causes, symptoms, and treatment
The term asthenia refers to physical weakness or a lack of energy. Asthenia can affect specific body parts, or it may affect the entire body.
[19]
Weakness and Fatigue - Clinical Methods - NCBI Bookshelf
Finally, these events may cause afferent impulses to reach the brain that are interpreted as weakness and fatigue. Go to: Clinical Significance. Feeling weak or ...
[20]
Weakness: MedlinePlus Medical Encyclopedia
Jul 23, 2024 · Weakness is reduced strength in one or more muscles. Causes Expand Section Weakness may be all over the body or in only one area.
[21]
Myasthenia Gravis: What It Is, Causes, Symptoms & Treatment
Myasthenia gravis is an autoimmune condition that causes skeletal muscle weakness. These are the muscles that connect to your bones and help you move.Myasthenia Gravis Treatment · Thymus · ThymectomyMissing: perceived based
[22]
Muscle Strength Testing - Physiopedia
The most commonly accepted method of evaluating muscle strength is the Oxford Scale (AKA Medical Research Council Manual Muscle Testing scale).
[23]
Diagnostic Approach to Proximal Myopathy - Skills in Rheumatology
Jan 6, 2021 · The distribution of weakness is mainly proximal in dermatomyositis and polymyositis, but as the disease progresses, distal muscles may become ...Clinical Presentation of... · Differential Diagnosis of... · Diagnostic Approach
[24]
CLINICAL APPROACH TO THE DIAGNOSTIC EVALUATION OF ...
Predominantly distal lower extremity weakness is highly suggestive of an acquired or inherited peripheral neuropathy, the differential for which is quite broad.
[25]
A Pattern Recognition Approach to Myopathy - PMC - PubMed Central
The distal arm/proximal leg pattern is associated with upper extremity weakness affecting the distal forearm muscles (wrist and finger flexors) and proximal ...
[26]
Acute stroke - PMC - NIH
Symptoms and signs of stroke. Anterior circulation strokes. Unilateral weakness. Unilateral sensory loss or inattention. Isolated dysarthria. Dysphasia. Vision ...<|control11|><|separator|>
[27]
Guillain-Barre syndrome - Symptoms and causes - Mayo Clinic
Jun 7, 2024 · People with Guillain-Barre syndrome usually experience their most significant weakness within two weeks after symptoms begin.
[28]
Current State and Future Directions in the Diagnosis of Amyotrophic ...
Considering its poor prognosis with a median survival time of 2 to 4 years and limited causal treatment options, an early diagnosis of ALS plays an essential ...
[29]
Fatigue in myasthenia gravis: is it more than muscular weakness?
Oct 3, 2013 · Myasthenia gravis (MG) is a chronic autoimmune disease that affects the neuromuscular junction, causing reduced muscular strength and reduced ...
[30]
A PATTERN RECOGNITION APPROACH TO THE PATIENT WITH A ...
Pattern 4: Distal Arm/Proximal Leg Weakness. This pattern is associated with distal arm weakness involving the distal forearm muscles (wrist and finger ...
[31]
Neuroanatomy, Upper Motor Neuron Lesion - StatPearls - NCBI - NIH
For example, left-sided lesions of the corticospinal tract in the spinal cord will cause left-sided weakness and spasticity. Unilateral UMN lesions ...
[32]
Upper Motor Neuron - an overview | ScienceDirect Topics
Spastic paralysis, hypertonia, and hyperreflexia have most often been associated with pyramidal tract damage, particularly lesions of the corticospinal tract.
[33]
Physical exercise-induced fatigue: the role of serotonergic and ...
Oct 19, 2017 · Brain serotonin and dopamine are neurotransmitters related to fatigue, a feeling that leads to reduced intensity or interruption of physical exercises.
[34]
The Dopamine Imbalance Hypothesis of Fatigue in ... - Frontiers
Mar 11, 2015 · Dopamine imbalance can be caused by changes in brain structure, particularly when structures critical for dopaminergic projections are damaged.
[35]
Serotonin and central nervous system fatigue: nutritional ...
Evidence is accumulating in support of a role for the neurotransmitter 5-HT, and perhaps dopamine, in central fatigue during prolonged exercise. Newsholme ...
[36]
Cerebellar Dysfunction - StatPearls - NCBI Bookshelf - NIH
May 6, 2024 · Cerebellar dysfunction causes balance problems and gait disorders along with difficulties in coordination, resulting in ataxia, ...
[37]
Ataxia - Physiopedia
Ataxia is usually caused by cerebellar dysfunction or impaired vestibular or proprioceptive afferent input to the cerebellum.Cerebellar Ataxia - A Case Study · Sensory Ataxia · Fragile X Tremor-Ataxia... · Edit
[38]
Motor Units and Muscle Receptors (Section 3, Chapter 1 ...
Because motor units are recruited in an orderly fashion, weak inputs onto motor neurons will cause only a few motor units to be active, resulting in a small ...
[39]
Neural Contributions to Muscle Fatigue: From the Brain to the ...
Peripheral fatigue is attributed to processes at or distal to the neuromuscular junction whereas central fatigue is attributed to processes within the nervous ...
[40]
Corticospinal Tract - Physiopedia
When the upper motor neurons of the corticospinal tract are damaged, it can lead to a collection of deficits sometimes called upper motor neuron syndrome. A ...
[41]
The Lower Motor Neuron Syndrome - Neuroscience - NCBI Bookshelf
A somewhat later effect is atrophy of the affected muscles due to denervation and disuse. The muscles involved may also exhibit fibrillations and fasciculations ...
[42]
Differentiating lower motor neuron syndromes
Lower motor neuron (LMN) syndromes are clinically characterised by muscle atrophy, weakness and hyporeflexia without sensory involvement.Late-Onset Sma · Spinobulbar Muscular Atrophy... · Motor Neuron DiseaseMissing: fiber | Show results with:fiber
[43]
Neuronal involvement in muscular atrophy - Frontiers
Muscular Atrophy Induced by Denervation. When muscle is denervated due to injury of lower motor neurons there ensues a flaccid paralysis and rapid atrophy ...
[44]
Axonal transport disruption in peripheral nerve disease
Abstract. Many neurodegenerative diseases and neuropathies have been proposed to be caused by a disruption of axonal transport.
[45]
The Neuromuscular Junction in Health and Disease - Frontiers
All CMSs present with fatigable muscle weakness, but age at onset, symptoms, distribution of weakness, and response to treatment vary, depending on the ...
[46]
Metabolic Myopathies - Medscape Reference
Sep 14, 2021 · Metabolic myopathies refer to a group of hereditary muscle disorders caused by specific enzymatic defects due to defective genes.
[47]
Biomolecules of Muscle Fatigue in Metabolic Myopathies - PMC
Dec 30, 2023 · This paper outlines the key biomolecules involved in muscle fatigue in metabolic myopathies, including energy substrates, enzymes, ion channels, and signaling ...
[48]
Duchenne muscular dystrophy | Nature Reviews Disease Primers
Feb 18, 2021 · Muscles without dystrophin are more sensitive to damage, resulting in progressive loss of muscle tissue and function, in addition to ...
[49]
Central and Peripheral Fatigue in Physical Exercise Explained
Mar 25, 2022 · Dopamine neurotransmission during exercise is a potential mechanism in inducing fatigue. For instance, a reduction in dopamine secretion ...
[50]
Role of exercise-induced potassium fluxes underlying muscle fatigue
Significant potassium flux from the intracellular space of contracting muscle may decrease the membrane potential to half its resting value. This is true for ...<|control11|><|separator|>
[51]
Acute Stroke Diagnosis - PMC - PubMed Central - NIH
Jul 1, 2009 · The most common presenting symptoms for ischemic stroke are difficulty with speech and weakness on one half of the body.
[52]
Hemiparesis | American Stroke Association
Apr 12, 2024 · Post-stroke paralysis symptoms They may include, but are not limited to: Hemiparesis (one-sided weakness); Spasticity/stiff muscles · Dysphagia ...Missing: focal | Show results with:focal
[53]
Ischemic Stroke - StatPearls - NCBI Bookshelf - NIH
Feb 21, 2025 · Additional symptoms include: Dysarthria, which is characterized by difficulty in phonation due to weakness of the facial muscles, lacks strong ...
[54]
Multiple Sclerosis - StatPearls - NCBI Bookshelf - NIH
Mar 20, 2024 · This condition manifests with a wide range of neurological symptoms, such as vision impairment, numbness and tingling, focal weakness, bladder ...
[55]
Multiple Sclerosis | National Institute of Neurological Disorders and ...
Jan 31, 2025 · Relapsing-remitting MS—Symptoms come in the form of recurrent attacks with total or partial recovery. The periods of disease inactivity ...
[56]
Amyotrophic Lateral Sclerosis - StatPearls - NCBI Bookshelf - NIH
ALS is a progressive neurodegenerative disorder that causes motor neuron degeneration and death, resulting in muscle weakness and respiratory failure.
[57]
DIABETIC NEUROPATHY PART 1: OVERVIEW AND SYMMETRIC ...
Various types of neuropathies can be associated with diabetes mellitus. 1 Symptoms usually include numbness, tingling, pain and weakness.
[58]
Chronic Inflammatory Demyelinating Polyradiculoneuropathy - NCBI
[1][2] Characterized by symmetric weakness in both proximal and distal muscles, CIDP is a subset of chronic acquired demyelinating polyneuropathies (CADP).
[59]
Polymyositis - Symptoms and causes - Mayo Clinic
Aug 10, 2022 · Polymyositis (pol-e-my-o-SY-tis) is an uncommon inflammatory disease that causes muscle weakness affecting both sides of your body.
[60]
Duchenne Muscular Dystrophy - StatPearls - NCBI Bookshelf
This manifests as toe walking, difficulty running, climbing up stairs, and frequently falling. Weakness is more pronounced in proximal than distal muscles and ...Continuing Education Activity · Introduction · Etiology · History and Physical
[61]
Polymyositis - StatPearls - NCBI Bookshelf
Feb 7, 2023 · Polymyositis, an autoimmune and chronic inflammatory myopathy, is characterized by symmetrical proximal muscle weakness due to the involvement of endomysial ...Introduction · History and Physical · Evaluation · Differential Diagnosis
[62]
Hypokalemic Periodic Paralysis - StatPearls - NCBI Bookshelf - NIH
Mar 19, 2024 · HypoPP is characterized by episodic severe muscle weakness, usually triggered by strenuous exercise or a high-carbohydrate diet.
[63]
Muscle Atrophy: Causes, Symptoms & Treatment - Cleveland Clinic
Symptoms include a decrease in muscle mass, one limb being smaller than the other, and numbness, weakness and tingling in your limbs. Disuse atrophy can be ...Overview · Symptoms And Causes · Management And Treatment
[64]
Skeletal Muscle Disuse Atrophy and the Rehabilitative Role of ...
Jul 1, 2020 · Muscle atrophy and weakness occur as a consequence of disuse after musculoskeletal injury (MSI). The slow recovery and persistence of these ...
[65]
Skeletal Muscle Wasting and Its Relationship With Osteoarthritis - NIH
Jun 15, 2019 · Progressive muscle weakness in OA is also associated with muscle fibre atrophy, with studies demonstrating 12–19% reduction in cross-sectional ...
[66]
Joint Pain and Weakness: Causes, Symptoms, and Treatment
May 3, 2024 · Common types of arthritis that can cause joint pain and muscle or ligament weakness include osteoarthritis and rheumatoid arthritis . Treatment ...
[67]
Factors affecting sarcopenia in older patients with chronic diseases
Mar 28, 2022 · Anemia, malnutrition, vitamin and trace element deficiencies, changes in hormone levels, and chronic inflammation are correlated with sarcopenia.
[68]
Hypothyroid Myopathy - StatPearls - NCBI Bookshelf
Jun 7, 2024 · ... generalized muscle weakness ... Muscle cramps: Hypothyroid myopathy can cause muscle cramps due to prolonged contraction of already weak muscles.Etiology · Pathophysiology · History and Physical · Toxicity and Adverse Effect...
[69]
Hypothyroidism (underactive thyroid) - Symptoms and causes
Dec 10, 2022 · Coarse hair and skin. Muscle weakness. Muscle aches, tenderness and stiffness. Menstrual cycles that are heavier than usual or irregular.Hypothyroidism and joint pain? · Hypothyroidism symptoms
[70]
Endocrine myopathies: clinical and histopathological features of the ...
Hyperthyroidism mainly leads to symptoms like muscle wasting and weakness such as proximal muscle weakness, involving both the upper and lower extremities, ...
[71]
Graves' Disease and the Manifestations of Thyrotoxicosis - NCBI - NIH
Sep 24, 2024 · The most common presenting symptoms are weight loss, weakness, dyspnea, palpitations, increased thirst or appetite, diarrhea, irritability, ...
[72]
An Overview of Post-viral Syndrome - Southern Medical Association
Aug 16, 2021 · These conditions frequently lead to a sense of tiredness and weakness, pain, difficulty concentrating and headaches that linger after the viral ...
[73]
Post-Viral Pain, Fatigue, and Sleep Disturbance Syndromes
PPS presents with muscle weakness, fatigue, myalgia, arthralgia, neuropathic pain, and functional decline 10 to 15 years after poliovirus infection. Myalgia and ...Post-Viral Pain · Post-Viral Fatigue · Post-Viral Sleep Disorders
[74]
Clinical Care and Treatment of Neurologic Lyme Disease - CDC
Mar 5, 2025 · ... weakness, facial palsy/droop (paralysis of the facial muscles) ... Peripheral nerve involvement: When the peripheral nerves are affected, patients ...
[75]
Lyme and neuropathy: How to ease nerve pain, tingling, and ...
Mar 9, 2021 · Severe sensitivity to touch; Worsening pain during nighttime; Muscle weakness; Loss of coordination in hands and feet. While this may feel like ...
[76]
Anemia - Symptoms and causes - Mayo Clinic
May 11, 2023 · Having anemia can cause tiredness, weakness and shortness of breath. ... Losing a lot of blood quickly causes severe anemia and can be fatal.Iron deficiency anemia · Aplastic anemia · Vitamin deficiency anemia · Thalassemia
[77]
What Is Anemia? - NHLBI - NIH
Mar 24, 2022 · If you have anemia, your body does not get enough oxygen-rich blood. The lack of oxygen can make you feel tired or weak.Iron-Deficiency · Vitamin B12–Deficiency Anemia · Hemolytic Anemia · Symptoms
[78]
Spinal Cord Subacute Combined Degeneration - StatPearls - NCBI
Apr 21, 2024 · Spinal cord SCD manifests with cognitive, motor, and sensory symptoms. This condition is most commonly caused by vitamin B12 deficiency.Continuing Education Activity · Introduction · Epidemiology · Evaluation
[79]
Subacute combined degeneration Information - Mount Sinai
SCD is caused by vitamin B12 deficiency. It mainly affects the spinal cord. But its effects on the brain and the peripheral (body) nerves are the reason for ...
[80]
Paraneoplastic syndromes of the nervous system - Mayo Clinic
Feb 20, 2024 · Symptoms include muscle weakness in the pelvis and legs, and fatigue. It also may cause trouble swallowing and speaking, irregular eye movement, ...
[81]
Paraneoplastic Syndromes - StatPearls - NCBI Bookshelf - NIH
Clinically LEMS is characterized by weakness of the proximal muscles predominantly affecting thigh and pelvic muscles; patients generally have difficulty in ...Continuing Education Activity · Pathophysiology · History and Physical · Evaluation
[82]
Cancer Cachexia: Symptoms, Treatment & Prognosis
Symptoms include significant weight loss, weakness and fatigue. It can be a life-threatening condition. Treatment focuses on nutrition, like eating small meals ...
[83]
Cachexia and Cancer - NCI
Oct 15, 2024 · Cancer cachexia is a wasting syndrome that leads to weakness, fatigue, and loss of skeletal muscle (also called sarcopenia) and fat.
[84]
How To Assess Sensation - Neurologic Disorders - Merck Manuals
The sensory examination is designed to localize dysfunction and help determine whether the problem is in the cerebral cortex, thalamus, sensory pathways in the ...
[85]
Stroke Symptoms and Warning Signs
Is the person's smile uneven? A = Arm Weakness – Is one arm weak or numb? Ask the person to raise both arms. Does one arm drift downward?Women and Stroke · Stroke survivor dances at... · The F.A.S.T. Experience
[86]
How ALS Is Diagnosed - Massachusetts General Hospital
Aug 1, 2018 · Muscle weakness, which is often only on one side of the body, such as one arm or one leg. · Vocal changes, especially slurred words or slow ...
[87]
Timed Up and Go Test: Purpose and Scoring - Medbridge
The Timed Up and Go test measures how long it takes to stand, walk 3 meters, turn, walk back, and sit from a chair. It evaluates balance and motor elements.
[88]
6 Minute Walk Test - Shirley Ryan AbilityLab
Aug 23, 2021 · The 6MWT assesses walking capacity by measuring the distance a patient walks in 6 minutes, self-paced with rests allowed.Missing: weakness | Show results with:weakness
[89]
Myasthenia Gravis - StatPearls - NCBI Bookshelf - NIH
The differential diagnosis for myasthenia gravis include the following: Lambert-Eaton syndrome is a fluctuating weakness that improves with exercise, ...
[90]
Differential diagnosis of idiopathic inflammatory myopathies in adults
Differential diagnosis of idiopathic inflammatory myopathies in adults – the first step when approaching a patient with muscle weakness · Toxic myopathies.Toxic Myopathies · Late-Onset Muscle... · Late-Onset Metabolic...<|control11|><|separator|>
[91]
https://www.mayoclinic.org/diseases-conditions/guillain-barre-syndrome/diagnosis-treatment/drc-20363006
[92]
None
### Key Steps for Initial Assessment: ABCs, Vital Signs, Stratification, Supportive Care, Monitoring in Acute Weakness (ENLS 5.0 Protocol)
[93]
[PDF] ESPEN guideline clinical nutrition in neurology
and dehydration may aggravate muscle weakness, contribute to respiratory ... diseases: the Neuromuscular Disease Swallowing Status Scale (NdSSS). J ...
[94]
Potential Therapeutic Strategies for Skeletal Muscle Atrophy - PMC
Exercise therapy is the most effective treatment for skeletal muscle atrophy. Unfortunately, it is not suitable for all patients, such as fractured patients and ...
[95]
Polymyositis Treatment & Management - Medscape Reference
Aug 14, 2025 · Immunosuppressants. Immunosuppressive agents are indicated in patients who do not improve with steroids within a reasonable period (ie, 4 wk) or ...Extramuscular Manifestations... · Inpatient and Outpatient Care
[96]
Treatment of idiopathic inflammatory myopathies - ScienceDirect.com
Current management relies on immunosuppressants like corticosteroids, methotrexate, azathioprine, mycophenolate mofetil, rituximab, and intravenous ...
[97]
Treatment of myasthenia gravis: focus on pyridostigmine - PubMed
Oct 1, 2011 · Pyridostigmine has been used as a treatment for MG for over 50 years and is generally considered safe. It is suitable as a long-term treatment.
[98]
Pyridostigmine (Mestinon): Uses & Side Effects - Cleveland Clinic
Pyridostigmine is a medication that treats myasthenia gravis. This condition causes muscle weakness that worsens throughout the day.
[99]
Guillain-Barre syndrome - Diagnosis and treatment - Mayo Clinic
Jun 7, 2024 · After the first symptoms, the condition tends to worsen for about two weeks. · Symptoms reach a plateau within four weeks. · Recovery begins, ...Symptoms and causes · Doctors and departments · Care at Mayo ClinicMissing: onset | Show results with:onset
[100]
A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
Mar 3, 1994 · Overall, riluzole therapy reduced mortality by 38.6 percent at 12 months and by 19.4 percent at 21 months (the end of the placebo-controlled ...Survival · Adverse Drug Reactions And... · Discussion
[101]
Riluzole for the treatment of amyotrophic lateral sclerosis - PubMed
Riluzole was approved by the US FDA in 1995 as the first drug to treat ALS. Although riluzole is generally safe and well tolerated in clinical practice, its ...
[102]
Resistance exercise training improves disuse-induced skeletal ...
Feb 7, 2025 · Resistance exercise training (RET) has been demonstrated as an effective countermeasure to prevent unloading-induced muscle atrophy and weakness ...
[103]
Resistance exercise training improves disuse-induced skeletal ...
Feb 7, 2025 · Resistance exercise training improves disuse-induced skeletal muscle atrophy in humans: a meta-analysis of randomized controlled trials.
[104]
Ankle‐foot orthoses for improving walking in people with calf muscle ...
Sep 20, 2021 · The mainstay of treatment to improve walking in people with calf muscle weakness is the provision of ankle‐foot‐orthoses (AFOs) (Hsu 2008).
[105]
Osteomalacia: What It Is, Symptoms & Treatment - Cleveland Clinic
Feb 20, 2025 · Osteomalacia treatment includes the use of vitamin D, calcium and/or phosphorus supplements. Your healthcare provider will tell you how much of ...
[106]
Osteomalacia and Vitamin D Status: A Clinical Update 2020 - PMC
Dec 21, 2020 · The goals of therapy for vitamin D‐deficiency osteomalacia are to alleviate symptoms, promote fracture healing, restore bone strength, and ...
[107]
Electrolytes - StatPearls - NCBI Bookshelf - NIH
Jul 24, 2023 · A patient that presents with weakness needs a basic electrolyte workup, as an electrolyte imbalance, especially in sodium and potassium levels, ...